Buffers for electrophoresis and use thereof

ABSTRACT

Various embodiments provide, for example, buffer compositions and/or sieving formulations useful in connection with electrophoresis instruments, such as capillary electrophoresis (CE) devices. In various embodiments, a buffer composition can include Bis-Tris, TAPS and/or TAPSO, and, optionally, a chelating agent, such as EDTA. Methods of separating samples containing bio-molecules, such as DNA or RNA, are also described.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No. 10/198,832, filed Jul. 19, 2002, which is a continuation-in-part of U.S. patent application Ser. No. 09/909,649, filed Jul. 19, 2001, the entireties of both of which are incorporated herein by reference.

BACKGROUND OF THE INVENTION

Electrophoresis is commonly used to separate biological molecules, such as deoxyribonucleic acid (“DNA”), ribonucleic acid (“RNA”), proteins, etc., according to size or length.

DNA base sequencing and fragment analysis are among the most useful embodiments of electrophoresis separations. In DNA base sequencing, for example, a DNA sequencing product is denatured and the resulting single stranded DNA sample is applied to an electrophoresis gel for separation.

Unfortunately, it is not uncommon to encounter sequencing errors involving specific sequences which are difficult to resolve. One such problem, called a “compression,” occurs when the single-stranded fragments anneal to themselves to form a “hairpin” structure at a particular position. The following schematic generally illustrates such an occurrence:

This may cause the fragment to migrate more quickly through the gel than one would expect from its length, which can result in bands that run very close together, sometimes overlapping one another.

FIELD OF THE INVENTION

The present teachings relate to buffer compositions and electrophoresis of biological molecules, such as nucleic acids.

SUMMARY OF THE INVENTION

The present teachings provide, among other things, buffer compositions and/or sieving (gel) formulations that improve the performance of electrophoresis instruments, such as capillary electrophoresis (CE) devices.

Various aspects provide a buffer composition for electrophoresis of nucleic acids. The buffer can be, for example, a running buffer.

In various embodiments, the buffer composition includes: (i) Bis-Tris; and (ii) one or more members of the group TAPS, TAPSO, and Asparagine. For example, the composition can comprise Bis-Tris as a cation and TAPS and/or TAPSO as an anion. Various embodiments further include EDTA as a metal chelator.

In various embodiments, the buffer composition includes: (i) TAPS, TAPSO, or Asparagine; and (ii) a compound of the formula: [HO(CH2)m]3C—N[(CH2)n-OH]2, wherein: m is an integer of from 1 to 3 (e.g., 1), and n is an integer of from 1 to 4 (e.g., 2).

The composition can include a metal-chelating agent, such as EDTA.

In some embodiments, the composition is substantially free of detergents, such as SDS.

In some embodiments, the composition has a pH greater than 7 (e.g., no less than 7.5). In some embodiments, the composition has a pH less than 8.

In various aspects, the present teachings provide a resolving-gel composition for electrophoresis of nucleic acids.

In various embodiments, the resolving-gel composition includes: (a) an organic polymer, (b) Bis-Tris, and (c) one or more members of the group TAPS, TAPSO, and Asparagine. For example, the composition can comprise Bis-Tris and TAPS and/or TAPSO.

In various embodiments, the composition is substantially detergent-free (e.g., free of SDS).

In some embodiments, the composition has a pH greater than 7 (e.g., no less than 7.5). In various embodiments, the composition has a pH less than 8.

Further aspects of the present teachings relate to apparatus for resolving samples.

In various embodiments, an apparatus includes: an anodic buffer (anolyte) chamber; a cathodic buffer (catholyte) chamber; an electrophoretic channel (e.g., a capillary tube having a lumen) extending between and communicating the anodic and cathodic buffer chambers; and a continuous buffer system comprising Bis-Tris held in the anodic and cathodic buffer chambers and in the channel.

In various embodiments, the continuous buffer system further comprises one or both of TAPS and TAPSO. For example, the buffer system can further comprise TAPS.

In some embodiments, the apparatus further includes a sieving medium (e.g., a gel or flowable (liquid-state) media) held in the channel.

Yet further aspects of the present teachings relate to methods of conducting electrophoresis of nucleic acids.

Various embodiments of such a method comprise: adding a buffer into an electrophoretic channel, wherein the buffer comprises Bis-Tris; adding a sample including nucleic acids to be analyzed into the channel; and resolving the sample by electrophoresis.

Various embodiments of a method of the present teachings comprise: (a) adding a buffer into an electrophoretic channel, wherein the buffer comprises a compound of the formula: [HO(CH2)m]3C—N[(CH2)n-OH]2, wherein m is an integer of from 1 to 3 (e.g., 1), and n is an integer of from 1 to 4 (e.g., 2); (b) adding a sample including nucleic acids to be analyzed (e.g., DNA or RNA) into the channel; and (c) resolving the sample by electrophoresis.

In various embodiments, a method of the present teachings comprises: introducing a buffer to a gel, wherein the buffer comprises Bis-Tris; applying a sample including nucleic acids to be analyzed (e.g., DNA or RNA) on the gel; and applying an electromotive potential difference across the gel, whereby the sample is resolved.

In various embodiments, the resolving is carried out at a pH of greater than 7 (e.g., no less than 7.5). In some embodiments, the resolving is carried out a pH of less than 8.

The teachings herein can be particularly useful in connection with channels (e.g., capillary tubes, or grooved plates) having cold zones; e.g., regions of at least 3, 4, 5 cm, or longer, that are not temperature-controlled (e.g., not disposed within a heating apparatus).

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic representation of a capillary electrophoresis (CE) device, useful in various embodiments.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

Reference will now be made to various non-limiting, exemplary embodiments. It will be understood that such embodiments are not intended to limit the present teachings. On the contrary, the present teachings are intended to cover alternatives, modifications, and equivalents, as will be appreciated by those skilled in the art.

Generally, the present teachings provide, among other things, compositions and methods that facilitate electrophoretic separation (e.g., provide for enhanced resolution).

Embodiments provide, for example, running buffers and/or sieving formulations (e.g., gels or flowable (liquid-state) media) that improve the performance of electrophoresis instruments, such as capillary electrophoresis (CE) devices. The present teachings are not limited, however, to CE devices. In various embodiments, the present teachings provide a composition comprising an electrolyte-containing buffer through which an electric current can be passed.

According to various embodiments, the present teachings provide a buffer for electrophoresis containing a cation configured such that the charge on the cation is hindered (e.g., sterically) from shielding the negative charges on the polynucleotides (e.g., DNA, RNA) of a sample. It has been discovered that such cations can assist in preventing renaturation of denatured DNA. Such effect can be particularly useful in electrophoresis apparatus having regions without means for temperature control, such as a heating assembly. Regions lacking temperature control means are sometimes referred to as “cold zones.”

A “cold zone” can be, for example, a region that is at or near ambient temperature during a run. Certain commercial sequencers may have one or more cold zones. For example, in some configurations, an ABI 310 instrument (Applied Biosystems) can include a first cold zone defined by a 6.6 cm region extending from an injection end of the capillary to the instrument's oven, and a second defined by a 3.8 cm region extending from the oven to the detector. In some configurations, an ABI 3100 instrument can include similarly situated cold zones at 4.8 cm and 4.5 cm, respectively. The present teachings can be useful, for example, in connection with such sequencers, among others.

Some embodiments of buffers of the present teachings contain the weak base Bis-Tris (bis[2-Hydroethyl]imino-tris[hydroxymethylmethane) as the cation. In aqueous solution, Bis-Tris molecules pick up protons to give the conjugate acid form, Bis-Tris+.

Bis-Tris is inert, easily prepared, and readily available from commercial sources (see Morin, L. G., Clin. Chem., 23, p. 1569 (1977); and Lewis, J. C., Anal. Biochem. 14, 495 (1966); each of which is incorporated herein by reference). Bis-Tris can be purchased, for example, from Research Organics (Cleveland, Ohio).

In various embodiments, a buffer composition includes (i) Bis-Tris, (ii) TAPS (N-tris[hydroxylmethyl]methyl-3-aminopropane-sulfonic acid), and optionally (iii) a chelating agent. Some formulations provided herein include (i) 100 mM Bis-Tris, (ii) 100 mM TAPS, and (iii) 1 mM EDTA (Ethylenediaminetetraacetic acid, pH 8).

In various embodiments, a buffer composition includes 50-200 mM Bis-Tris (e.g., 100 mM) in a 1:1 ratio with TAPS or TAPSO, and 1-2 mM EDTA. In some embodiments, a buffer comprises 50 mM BisTris, 50 mM TAPSO, and 2 mM EDTA.

In various of the formulations described herein, TAPSO, 3-[N-tris(hydoxymethyl)methylamino]-2-hydroxypropanesufonic acid, can be substituted for TAPS, or included in addition thereto. Further, Asparagine can be substituted for TAPS in the buffer.

In various embodiments, molecules comprising the following are included in a buffer composition: [HO(CH₂)_(m)]₃C—N[(CH₂)_(n)—OH]₂, with m=1, 2, 3, . . . m (integral), n=1, 2, 3, . . . n (integral), e.g., m=1 to 3 and n=1 to 4, or e.g., m=1 and n=2.

The present teachings provide, in part, gel or flowable separation media compositions for electrophoresis. In various embodiments, a resolving gel composition includes: (a) one or more organic polymers and (b) Bis-Tris. In some embodiments, gel compositions according to the presents teachings further include one or more members of the group TAPS, TAPSO, and Asparagine. In various embodiments, the gel composition includes TAPS and/or TAPSO.

According to various embodiments, a buffer composition is included in a sieving medium (e.g., a gel or flowable separation media); such as the sieving mediums described in U.S. Pat. No. 5,126,021, and WO 02/24313, each of which is incorporated herein by reference.

A composition according to the present teachings can include, for example, a sieving component and a surface interaction component, such as described, for example, in WO 02/24313; incorporated herein by reference.

In various embodiments, the sieving component of the composition contains one or more noncrosslinked acrylamide polymers. Noncrosslinked acrylamide polymers may include, for example, linear polymers such as polyacrylamide (LPA), branched polymers, and star-shaped polymers.

In various embodiments, the surface interaction component of the compositions comprises one or more uncharged and uncrosslinked water-soluble silica-adsorbing polymer. Such compontents may belong to a variety of chemical classes, such as those described in the following references: Molyneux, Water-Soluble Synthetic Polymers: Properties and Behavior, Volumes I and II (CRC Press, Boca Raton, 1982); Davidson, Editor, Handbook of Water-Soluble Gums and Resins (McGraw-Hill, New York, 1980); Franks, editor, Water: A Comprehensive Treatise (Plenum Press, New York, 1973); and the like. The uncharged water-soluble silica-adsorbing polymers of the present teachings can include, but are not limited to, N,N-disubstituted polyacrylamides, N-monosubstituted polyacrylamides, polymethacrylamide, polyvinylpyrrolidone, and the like. In some embodiments, the surface interaction component comprises poly(N,N-dimethylacrylamide) (pDMA).

In various embodiments, polymers of a composition of the present teachings are selected from the group consisting of polyvinylactams, such as polyvinylpyrrolidone; N,N-disubstituted polyacrylamides; and N-substituted polyacrylamides.

Various polymers that can be included in a composition of the present teachings include, but are not limited to, those disclosed in U.S. Pat. No. 5,552,028, U.S. Pat. No. 5,567,292, U.S. Pat. No. 6,387,234; WO 02/24313; H. He et al., Electrophoresis 2002, 23, 1421-1428; and M. N. Albarghouthi et al., Electrophoresis 2001, 22, 737-747; Liguo Song et al., Electrophoresis 2001, 22, 729-736; Dehai Liang et al., Electrophoresis 2000, 21, 3600-3608; each of which is incorporated herein by reference.

Capillary electrophoresis can be performed, for example, using any suitable capillaries, e.g., fused silica capillary tubes, or grooves formed in glass or plastic plates, or in chips. Various embodiments, for example, contemplate the use of elongate tubes, each having an inner diameter, for example, within a range of about 10 to 500 microns, e.g., no greater than about 100 microns. Optionally, each tube can be coated on its outer surfaces along its length with an opaque polyimide coating to prevent breakage. In some embodiments, the separation is performed by filling the capillary tube with only a buffer solution, while in other cases a sieving medium (e.g., polymer or gel) is added, as well. In an exemplary process, a sample is introduced into the inlet end of the capillary tube and an electric field applied. Under the influence of the electric field, the sample separates, causing the individual components to migrate down the length of the capillary tube. At or near the outlet end of the capillary tube, a small region of the opaque polyimide coating can be removed to form an optical detection region. The individual components can be detected using, for example, fluorescence or ultraviolet absorbance.

Details of common features of an operable capillary electrophoresis device may be found in any number of available publications, e.g., Capillary Electrophoresis Theory and Practice, Grossman and Colbum, eds., Academic Press (1992), incorporated herein by reference.

According to various embodiments, a buffer in accordance with the present teachings is employed in electrophoretic separations of nucleic acids using a ABI Prism 310 or ABI Prism 3100 sequencing apparatus (Applied Biosystems; Foster City, Calif.).

In various embodiments, a buffer according to the present teachings is employed in a “continuous buffer system.” That is, in a system wherein the same buffer of a chosen pH and ionic strength is used in a sieving medium (gel or flowable medium) and in the anode and cathode buffer chambers. FIG. 1, for example, shows a CE device including a cathode buffer reservoir 12, an anode buffer reservoir 14, and a channel defined by a capillary tube 16 extending between the cathode and anode buffer reservoirs. A sieving medium can be held in the channel. A continuous buffer system can be provided by including in both the anode and cathode buffer reservoirs, as well as in the channel, a buffer composition of the present teachings. A sample, loaded into the channel, can be resolved by applying an electromotive potential across the channel by way of an appropriate power source 20. Separated components of the sample can be detected by way of a suitable detection/data-collection assembly 22.

In various embodiments, a Bis-TrisTAPS buffer composition is included in both the cathodic and anodic buffer chambers of a CE apparatus, as well as in a sieving medium (e.g., a resolving gel or flowable medium) held in one or more capillaries of the apparatus. One or more polynucleotide-containing samples can then be resolved using the apparatus, so prepared.

In various embodiments, separation of a nucleic acid-containing sample is effected at a pH of at least 7, of greater than 7, and/or at least 7.5. In some embodiments, separation is effected at a pH of 8, or less.

The following examples are intended for illustration purposes only, and should not be construed as limiting in any way.

EXAMPLE 1

A buffer solution in accordance with the present teachings was formulated as: 100 mM Bis-Tris (bis[2-Hydroethyl]imino-tris[hydroxymethylmethane), 100 mM TAPS (N-tris[hydroxylmethyl]methyl-3-aminopropane-sulfonic acid), and 1 mM EDTA (Ethylenediaminetetraacetic acid, pH 8).

1 mM EDTA was used to eliminate or alleviate damage to the capillary coating due to metals.

EXAMPLE 2

Less temperature induced DNA band broadening was observed with TrisTAPS than with NaTAPS (Tris-(hydroxymethyl)-methyl-amino-propanesulfonic acid, sodium salt) running buffer. To understand how the cations, Tris and Na, influence DNA band broadening during electrophoresis, DNA separation and mobility were examined during capillary electrophoresis with running buffers containing the different metal cations: Li, Rb, Ca, Mg, K, and Cs; and organic buffers, Bis-Tris, TrisBispropane, imidizole, arginine, ammonium, and tetrapentylammonium. It was noticed that the sizing of a fragment, referred to herein as GS700 250 nucleotide (nt) fragment, or simply the 250 nt fragment, which has putative DNA secondary structure that causes it to run anomalously under low DNA denaturant conditions, was running near its predicated size (250 nt) with Bis-TrisTAPS as the running buffer during capillary electrophoresis. From an examination of the structure of the Bis-Tris molecule, it is believed that Bis-Tris may be sterically hindered from shielding the negative ions on the DNA backbone, thereby reducing its ability to renature during electrophoresis.

EXAMPLE 3

The ability of the buffer of the present teachings to improve nucleic acid denaturation during electrophoresis was observed in the following assays:

EXAMPLE 3(A)

One assay measured the ability of the present buffer to reduce the anomalous mobility of the GS700 250 nucleotide (nt) fragment—the anomalous mobility is thought to be due to DNA secondary structure. The results from this assay are reported in Table I. During electrophoresis at 70° C. on the ABI Prism 310 instrument using POP37 polymer (Applied Biosystems; Foster City, Calif.), with TrisTAPS as the running buffer, the 250 nt fragment migrated as 244.5 nt, and with an additional IM urea in the polymer formulation, the 250 nt fragment migrated as 245.5 nt. Using Bis-Tris buffer (without additional urea) the 250 nt fragment migrated as a 247.5 nt fragment—closer to the correct 250 nt than obtained by adding an additional 1 M urea to the polymer. TABLE I Migration of the 250 nt fragment buffer cation 50° C. 60° C. 70° C. Na 241.7 ND 244.9 Tris 242.7 ND 244.5 Tris + 1 M urea* 244.8 244.7 245.5 Bis-Tris 246.0 247.0 247.4 *additional urea added to polymer formulation

EXAMPLE 3(B)

Second, the ability to reduce the severity of a 4 base compression, CGCC, was measured. The spacing of the C terminated fragments flanking the compression were measured and then the deviation of the C nucleotides in the compression from the normal spaces was calculated. Completely normal spacing or no compression would result in “0” deviation. The less the DNA is denatured, the greater compression, and, therefore, the larger the deviation of the 3 C nucleotides from normal. Table II shows the smallest deviation with Bis-Tris buffer, and once again more denaturation is seen with the switch to Bis-Tris buffer than with the addition of an extra 1 M urea. TABLE II buffer cation temp. (° C.) C base scan # y-inter slope cal base difference sum dev. Bis-Tris 60 10 3123 3011.4 10.5 10.62857 0.628571 2.847619 12 3131 3011.4 10.5 11.39048 0.609524 13 3131 3011.4 10.5 11.39048 1.609524 65 10 3006 2898.8 10.31 10.39767 0.397672 2.662464 12 3016 2898.8 10.31 11.3676 0.632396 13 3016 2898.8 10.31 11.3676 1.632396 70 10 2999 2888.8 10.57 10.42573 0.425733 2.492904 12 3010 2888.8 10.57 11.46641 0.533586 13 3010 2888.8 10.57 11.46641 1.533586 Tris 60 10 3502 3394 9.76 11.06557 1.065574 3.934426 12 3502 3394 9.76 11.06557 0.934426 13 3502 3394 9.76 11.06557 1.934426 65 10 3338 3231.3 9.54 11.18449 1.184486 3.815514 12 3338 3231.3 9.54 11.18449 0.815514 13 3338 3231.3 9.54 11.18449 1.815514 70 10 3151 3047.3 9.22 11.24729 1.247289 3.752711 12 3151 3047.3 9.22 11.24729 0.752711 13 3151 3047.3 9.22 11.24729 1.752711 Na 60 10 3487 3377.6 10.02 10.91816 0.918164 4.081836 12 3487 3377.6 10.02 10.91816 1.081836 13 3487 3377.6 10.02 10.91816 2.081836 65 10 3408 3292.4 10.315 11.20698 1.20698 3.79302 12 3408 3292.4 10.315 11.20698 0.79302 13 3408 3292.4 10.315 11.20698 1.79302 70 10 3338 3223.8 10.154 11.2468 1.246799 3.753201 12 3338 3223.8 10.154 11.2468 0.753201 13 3338 3223.8 10.154 11.2468 1.753201 Tris + 1 M 60 10 4191 4067.7 11.01 11.19891 1.19891 3.80109 urea* 12 4191 4067.7 11.01 11.19891 0.80109 13 4191 4067.7 11.01 11.19891 1.80109 65 10 3968 3846.9 10.655 11.36556 1.365556 3.634444 12 3968 3846.9 10.655 11.36556 0.634444 13 3968 3846.9 10.655 11.36556 1.634444 70 10 3730 3625 9.8 10.71429 0.714286 3.265306 12 3735 3625 9.8 11.22449 0.77551 13 3735 3625 9.8 11.22449 1.77551 *The polymer was formulated with an additional 1 M urea.

It will be appreciated that various embodiments of the present teachings provide running buffers useful, for example, in capillary electrophoresis of DNA, especially when increased DNA denaturation is desired. Embodiments of the present teachings can provide for increased DNA denaturation during electrophoresis, without significant loss of DNA resolution or run speed, which is commonly observed with extra chemical denaturants such as urea or 2-pyrrolidinone.

Optionally, the compositions and methods described herein can be employed in combination with other methods aimed at alleviating or minimizing compressions. For example, one method involves sequencing of the other strand, as the factors contributing to the secondary structure are often not found on the complementary strand. Another strategy to eliminate compressions is to include organic solvents such as formamide and/or urea in an attempt to reduce the amount of base pairing. Yet a further strategy is to lower the stability of the secondary structures in the product strand by substituting ITP or 7-deaza-dGTP for GTP. Also, heat can be used in to disrupt hydrogen bonds resulting in denatured DNA and RNA.

Although the present teachings have been described with reference to various applications, methods, and compositions, it will be appreciated that various changes and modifications may be made without departing from the spirit hereof. The foregoing examples are provided to further illustrate the present teachings and are not intended as limiting. 

1. A method for increasing an amount of DNA denaturation that occurs during electrophoresis of nucleic acids without significant loss of DNA resolution or run speed, said method comprising: introducing a buffer to a gel, wherein said buffer comprises Bis-Tris, TAPS, and a metal-chelating agent, wherein said buffer lacks urea; applying a sample including nucleic acids to be analyzed on said gel; and applying an electromotive potential across the gel, whereby there is less loss of DNA resolution or run speed than if urea had been included in the buffer instead of the combination of Bis-Tris and TAPS.
 2. The method of claim 2, wherein the gel is supported in a channel defined by a capillary tube.
 3. The method of claim 2, wherein a pH of the buffer is at least
 7. 4. The method of claim 2, wherein a pH of the buffer is no less than 7.5.
 5. A method for facilitating an amount of DNA denaturation at a given temperature during electrophoresis, said method comprising: introducing a buffer to a gel, wherein said buffer comprises Bis-Tris and TAPS; applying a sample including nucleic acids to be analyzed on said gel; applying a temperature of at least 50° C. to the gel; and applying an electromotive potential across the gel, whereby an amount of denaturation that occurs at 50° C. in the buffer is greater than an amount of denaturation of the nucleic acids in a buffer having Tris but excluding Bis-Tris at a temperature of at least 60° C.
 6. The method of claim 5, wherein the amount of denaturation that occurs at 50° C. in the buffer is greater than an amount of denaturation of the nucleic acids in a buffer having Tris but excluding Bis-Tris at a temperature of 70° C.
 7. The method of claim 5, wherein a pH of the buffer is no less than 7.5.
 8. A method for increasing an amount of DNA denaturation that occurs during electrophoresis comprising: identifying a sample as having nucleic acids that could benefit from an increased amount of denaturation during electrophoresis; introducing a buffer to a gel, wherein said buffer comprises at least Bis-Tris and TAPS; applying the sample including nucleic acids to be analyzed on said gel; and applying an electromotive potential across the gel.
 9. The method of claim 8, wherein the electrophoresis is capillary electrophoresis.
 10. The method of claim 8, wherein a pH of the buffer is no less than 7.5.
 11. The method of claim 8, wherein, despite the increase in denaturation, said nucleic acid runs without a significant loss of DNA resolution or run speed when the electromotive potential is applied across the gel because urea is not present in the buffer.
 12. A method for decreasing compression that occurs during electrophoresis of nucleic acids comprising: identifying a sample as having nucleic acids that could benefit from a decreased amount of compression during electrophoresis; introducing a buffer to a gel, wherein said buffer comprises at least Bis-Tris and TAPS; applying the sample including nucleic acids to be analyzed on said gel; and applying an electromotive potential across the gel.
 13. The method of claim 12, wherein the buffer further comprises an organic solvent.
 14. The method of claim 12, wherein the buffer further comprises formamide, urea, or both formamide and urea.
 15. The method of claim 12, wherein a pH of the buffer is no less than 7.5.
 16. A method for the electrophoresis of nucleic acids, comprising: introducing a buffer to a gel, wherein said buffer comprises Bis-Tris, TAPS, and a metal-chelating agent; applying a sample including nucleic acids to be analyzed on said gel; and applying an electromotive potential difference across said gel, whereby the sample is resolved, wherein the gel is supported in a channel defined by a capillary tube comprising a cold zone, wherein an amount of compression that occurs from resolving the sample by electrophoresis through the capillary tube is less than an amount that occurs in a Tris buffer that lacks Bis-Tris.
 17. A method for gel electrophoresis, said method comprising: introducing a buffer to a gel in order to increase an amount of DNA denaturation or decrease an amount of compression that would occur in nucleic acids to be analyzed in the gel, said buffer comprising Bis-Tris, TAPS, and a metal-chelating agent; applying a sample including nucleic acids to be analyzed on said gel; and applying an electromotive potential across the gel.
 18. A composition for electrophoresis of nucleic acids, the composition comprising: (a) an organic polymer, (b) Bis-Tris, (c) one or more members of the group TAPS, TAPSO, and Asparagine; and (d) a metal-chelating agent, wherein the organic polymer comprises a sieving component comprising a non-crosslinked acrylamide polymer, and a surface interaction component comprising one or more non-crosslinked polymers selected from the group consisting of N,N-disubstituted polyacrylamide, N-substituted polyacrylamide, N-monosubstituted polyacrylamides, polymethacrylamide, polyvinylpyrrolidone, and poly(N,N-dimethylacrylamide), and wherein the resolving-gel composition has a pH of greater than
 7. 19. The composition of claim 18, comprising TAPS, and wherein the gel is contained within an electrophoretic capillary.
 20. The composition of claim 18, having a pH no less than 7.5.
 21. The composition of claim 18, wherein the non-crosslinked acrylamide polymer is selected from the group consisting of: linear polyacrylamide, branched acrylamide polymers, and star-shaped acrylamide polymers. 